Gel composition for treating mycosis

a gel composition and mycosis technology, applied in the direction of biocide, heterocyclic compound active ingredients, aerosol delivery, etc., can solve the problems of reducing patient compliance, affecting the treatment effect of patients, and requiring 3 to 6 months of nail turnover for oral treatment, etc., to achieve excellent absorption and permeation of kp-103 and good storage stability.

Active Publication Date: 2014-11-18
KAKEN PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0006]An object of the present invention is to provide an external therapeutic preparation for mycoses, which is excellent in absorption and permeation of KP-103 at a target site (skin and nail). Another object of the present invention is to provide a preparation, which ensures good storage stability of KP-103.Means for Solving the Problems
[0008]Thus, when compared to conventional solutions, the KP-103 gel composition of the present invention is excellent in drug permeation at a target site, particularly also excellent in permeation into the nail, and produces a therapeutic effect even on mycoses caused by fungi in the nail within a short period of time.

Problems solved by technology

Particularly in the treatment of onychomycoses, oral antifungal preparations are mainly used because existing antifungal preparations for external use cannot achieve sufficient drug permeation into the thick keratin layer in the nail plate and hence cannot produce any antifungal effect on fungi in the nail.
However, treatment via the oral route requires 3 to 6 months in terms of nail turnover.
This significantly reduces the compliance of patients.
However, such external preparations for superficial mycoses with enhanced permeation have been difficult to develop.
Particularly in the case of external preparations for onychomycoses, the same permeation effect as observed in the skin cannot apply to the nail because of differences in chemical structure between nail and skin.
Thus, it has been difficult to improve drug permeation in the nail.

Method used

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  • Gel composition for treating mycosis
  • Gel composition for treating mycosis
  • Gel composition for treating mycosis

Examples

Experimental program
Comparison scheme
Effect test

examples 1 to 5

[0064]In Examples 1 to 5 shown below, individual ingredients were mixed to prepare a gel composition according to the following formula. First, among the ingredients, KP-103 was dissolved in ethanol. To this solution, triacetin, glycerine (and 1,3-butylene glycol) were added and mixed, followed by addition of carboxyvinyl polymer. The mixture was warmed to disperse the carboxyvinyl polymer. After cooling, diisopropanolamine was added to prepare a gel composition. The carboxyvinyl polymer used was Hiviswako® 104, which is a product of Wako Pure Chemical Industries, Ltd., Japan. To measure the pH of each gel composition, 0.1 g of the gel composition was diluted in 5 mL water and measured with a pH meter (F-23, Horiba, Ltd., Japan).

[0065]Based on the mass of the whole composition to be prepared, which was set to 100 g, individual ingredients were mixed at the ratio indicated below to prepare the composition (gel preparation) of Example 1 according to the present invention.

[0066]

TABLE 1...

examples 6 to 11

[0081]Compositions (gel preparations) were prepared based on the formula used in Example 4 by varying the amount of KP-103 and the type of carboxyvinyl polymer as indicated in the table below. Carbopol® 940 is a product of Noveon, Inc. and Synthalen® K is a product of 3V SIGMA.

[0082]

TABLE 6Example 6Example 7Example 8Example 9Example 10Example 11KP-103 1 g 3 g 3 g 5 g 5 g 5 gCarboxyvinyl 1 g 1 g 1 g 1 g 1 g 1 gpolymer(Carbopol(Hiviswako(Carbopol(Hiviswako(Carbopol(Synthalen(trade name)940)104)940)104)940)K)Triacetin15 g15 g15 g15 g15 g15 gAnhydrous ethanolq.s.q.s.q.s.q.s.q.s.q.s.Concentrated35 g35 g35 g35 g35 g35 gglycerin1,3-Butylene glycol25 g25 g25 g25 g25 g25 gDiisopropanolamine0.2 g 0.2 g 0.2 g 0.2 g 0.2 g 0.2 g Tocopherol0.01 g  0.03 g  0.03 g  0.05 g  0.05 g  0.05 g  

examples 12 to 15

[0083]Compositions (gel preparations) were prepared based on the formula used in Example 4 by varying the amounts of polyhydric alcohols, except for concentrated glycerin, as indicated in the table below.

[0084]

TABLE 7Example 12Example 13Example 14Example 15KP-103 1 g 1 g 1 g 1 gCarboxyvinyl polymer 1 g 1 g 1 g 1 g(trade name)(Hiviswako 104)(Hiviswako 104)(Hiviswako 104)(Hiviswako 104)Triacetin15 g15 g15 g15 gAnhydrous ethanolq.s.q.s.q.s.q.s.Concentrated glycerin35 g35 g35 g35 g1,3-Butylene glycol 5 g—15 g—Dipropylene glycol20 g20 g—15 gTriethylene glycol— 5 g10 g10 gTocopherol0.2 g 0.2 g 0.2 g 0.2 g 

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Abstract

The present invention provides a stable gel composition for mycosis treatment, with increased absorption and permeation of (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidin -1-yl)-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol into a target site (skin and nail). The gel composition for mycosis treatment, comprises (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidin-1-yl) -1-(1H-1,2,4-triazol-1-yl)-butan-2-ol or an acid addition salt thereof, a lower alcohol, a polyhydric alcohol and a gel-forming polymer. The gel composition of the present invention increases permeation of the above compound into a target site and into the nail. The gel composition of the present invention allows the drug to be directly and rapidly absorbed and permeated into a target site in a constant manner, for mycosis treatment, particularly onychomycosis treatment.

Description

TECHNICAL FIELD[0001]The present invention relates to a gel composition for mycosis treatment, which ensures good absorption and permeation of (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylenepiperidin-1-yl)-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol (hereinafter also abbreviated as “KP-103”) into the skin and nail. The present invention also relates to a gel composition for mycosis treatment, which is excellent in storage stability of this drug.BACKGROUND ART[0002]In the case of external preparations for treatment of superficial mycoses, their therapeutic effect is greatly influenced by each drug's ability to permeate the skin and nail. Particularly in the treatment of onychomycoses, oral antifungal preparations are mainly used because existing antifungal preparations for external use cannot achieve sufficient drug permeation into the thick keratin layer in the nail plate and hence cannot produce any antifungal effect on fungi in the nail. However, treatment via the oral route requires 3 to ...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): A61K47/10A61K47/14A61K9/00A61K47/32A61K31/454A61K9/06A61K47/26
CPCA61K47/10A61K47/26A61K9/06A61K31/454A61K9/0014A61K47/14A61K47/32A61P31/10
Inventor OKUMURA, TOMOHIROOCHIAI, AKIKOSAKUDA, KEIZOTATSUMI, YOSHIYUKI
Owner KAKEN PHARMA CO LTD
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